Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractVolatile aroma composition of distillates produced from fermented sweet and acid whey    Next AbstractQuantification of re-evaporated mass from loaded fibre-mist eliminators »

Mol Genet Genomics


Title:Regulation of bacteriocin production in Lactobacillus plantarum depends on a conserved promoter arrangement with consensus binding sequence
Author(s):Risoen PA; Johnsborg O; Diep DB; Hamoen L; Venema G; Nes IF;
Address:"Department of Chemistry and Biotechnology, Agricultural University of Norway, As"
Journal Title:Mol Genet Genomics
Year:2001
Volume:265
Issue:1
Page Number:198 - 206
DOI: 10.1007/s004380000397
ISSN/ISBN:1617-4615 (Print) 1617-4623 (Linking)
Abstract:"Bacteriocin production in Lactobacillus plantarum C11 is regulated by a three-component signal transduction system comprising a peptide pheromone (PlnA), a histidine protein kinase (PlnB), and two homologous response regulators (RRs; PlnC and PlnD). Both RRs are DNA-binding proteins that bind to promoter-proximal elements in the pln regulon. The binding site for the two regulators consists of two 9-bp direct repeats, that conform to the consensus sequence 5'-TACGTTAAT-3', and the repeats are separated by an intervening 12-bp AT-rich spacer region. In the present work, the plhA promoter was used as a model to evaluate the significance of the binding sequence and conserved promoter arrangement. Point substitutions in the consensus sequence, particularly those in invariant positions, either abolished or significantly reduced binding of PlnC and PlnD. Both regulators bind as homodimers to DNA fragments containing a complete set of regulatory elements, while removal of either repeat, or alterations in the length of the spacer region, significantly weakened binding of both protein dimers. DNase I footprinting demonstrated that PlnC and PlnD both bind to, and protect, the direct repeats. By fusing the plnA promoter region to the beta-glucuronidase (GUS) gene, it was shown that promoter activity is dependent on an intact set of accurately organized repeats. The in vitro and in vivo results presented here confirm the involvement of the repeats as regulatory elements in the regulation of bacteriocin production"
Keywords:"Bacteriocins/biosynthesis/*genetics/metabolism Base Sequence *Consensus Sequence DNA Footprinting DNA, Bacterial/analysis Deoxyribonuclease I *Gene Expression Regulation, Bacterial Genes, Reporter Glucuronidase/genetics/metabolism Lactobacillus/*genetics/;"
Notes:"MedlineRisoen, P A Johnsborg, O Diep, D B Hamoen, L Venema, G Nes, I F eng Research Support, Non-U.S. Gov't Germany 2001/05/24 Mol Genet Genomics. 2001 Mar; 265(1):198-206. doi: 10.1007/s004380000397"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 06-11-2024